Infectious Diseases and Tropical Medicine Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Department of Microbiology, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Curr Microbiol. 2022 Aug 10;79(9):285. doi: 10.1007/s00284-022-02976-5.
The present study aimed to investigate the mechanisms of resistance to tigecycline and to determine sequence types of Acinetobacter baumannii isolates recovered from children, using the Multilocus Sequence Typing (MLST). A total of 74 A. baumannii isolates were recovered from patients at one of the children's hospital in Tehran, Iran. Antimicrobial susceptibility testing of the isolates was performed for different classes of antibiotics and minimum inhibitory concentrations of colistin and tigecycline were determined using broth microdilution method and E-test strips, respectively. The presence of ISAba1, AbaR, tet(39), and tetX and the expressions of adeB, adeG, and adeJ efflux pump genes were measured using Polymerase Chain Reaction (PCR) and quantitative real-time PCR (RT-PCR), respectively. The diversity of mutations across the regulatory genes of RND efflux pumps (adeRS, adeL, and adeN) and trm gene were determined using their PCR amplification and DNA sequencing in tigecycline-resistant isolates. In addition, STs of tigecycline-resistant isolates were determined using MLST method. Three A. baumannii isolates were resistant to tigecycline. Several amino acid substitutions were identified in AdeRS, AdeN, and Trm but no alteration was found in AdeL. Nevertheless, adeB, adeG, and adeJ overexpression were observed in 1, 2, and 1 isolates, respectively. The tigecycline-resistant isolates belonged to ST1720 and ST2285. This is the first study reporting on ST2285 in A. baumannii populations. Among 74 isolates, two tigecycline susceptible isolates carried tet(39) gene but no tetX gene was detected. We concluded that mutations in regulatory genes of RND efflux pumps and the trm gene may play some important role in A. baumannii resistance to tigecycline.
本研究旨在通过多位点序列分型(MLST)研究对替加环素耐药机制进行研究,并确定从伊朗德黑兰一家儿童医院的患者中分离出的鲍曼不动杆菌分离株的序列类型。从伊朗德黑兰的一家儿童医院的患者中分离出了 74 株鲍曼不动杆菌。采用肉汤微量稀释法和 E 试验条测定了分离株对不同类别的抗生素的药敏试验和最低抑菌浓度(MIC),并分别测定了多粘菌素和替加环素的最小抑菌浓度。采用聚合酶链反应(PCR)和实时定量 PCR(RT-PCR)法分别检测 ISAba1、AbaR、tet(39)、tetX 及 adeB、adeG 和 adeJ 外排泵基因的表达。采用 PCR 扩增和 DNA 测序法测定了 RND 外排泵(adeRS、adeL 和 adeN)调节基因和 trm 基因的突变多样性。此外,还采用 MLST 方法确定了耐替加环素的分离株的 ST。有 3 株鲍曼不动杆菌对替加环素耐药。在 AdeRS、AdeN 和 Trm 中鉴定出几个氨基酸取代,但在 AdeL 中未发现任何改变。然而,在 1、2 和 1 株分离株中观察到 adeB、adeG 和 adeJ 过表达。耐替加环素的分离株属于 ST1720 和 ST2285。这是首次报道鲍曼不动杆菌种群中的 ST2285。在 74 株分离株中,有 2 株替加环素敏感株携带 tet(39)基因,但未检测到 tetX 基因。我们得出结论,RND 外排泵调节基因和 trm 基因的突变可能在鲍曼不动杆菌对替加环素的耐药性中起重要作用。